chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
724359372435938GC29GENIChomozygous115545099
724363412436342CG14GENIChomozygous115976510
724363422436343GC14GENIChomozygous116268450
724398532439854TG7GENIChomozygous115545101
724398572439858TG7GENIChomozygous115545103
724398812439882AG12GENIChomozygous115545105
724401382440139AG20GENIChomozygous115545107
724401942440195AC21GENIChomozygous115545109
724403012440302GA23GENIChomozygous115545111
724405212440522GC22GENIChomozygous115545113
724405362440537GA27GENIChomozygous115545115
724410442441045TC23GENIChomozygous115545117
724411382441139AG23GENICpossibly homozygous118391810
724411402441141AG31GENICpossibly homozygous118391811
724414382441439TA17GENIChomozygous115545119
724416962441697GA15GENIChomozygous115545121
724423202442321CT14GENIChomozygous115545123
724427792442780CT19GENIChomozygous115545125
724461352446136GA31GENIChomozygous115545137
724465292446530TC33GENIChomozygous115545139
724480032448004CA29GENIChomozygous115545141
724490592449060GA28GENIChomozygous115545145
724491552449156GA16GENIChomozygous115545147
724493292449330TC16GENIChomozygous115545149
724494452449446AG30GENIChomozygous115545151
724497362449737CG27GENIChomozygous115545153
724499132449914GA26GENIChomozygous115545155
724501252450126TC26GENIChomozygous115545157
724503222450323TC19GENIChomozygous115545159